Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Marie-Noelle Roy"'
Publikováno v:
Synthesis. 2011:2275-2280
Tetraarylphosphonium (TAP)-supported phosphorus ylides were prepared and used in copper-catalyzed olefination reactions with diazo compounds to produce conjugated esters, amides, and phosphonates. The TAP-phosphine oxide can easily be separated from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9607b1c2afd2889001de02812b38cfa6
https://doi.org/10.1055/s-0030-1260065
https://doi.org/10.1055/s-0030-1260065
Publikováno v:
Copper-Catalyzed Asymmetric Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20318d5fe69f424713bb13e38bd72418
https://doi.org/10.1002/9783527664573.ch8
https://doi.org/10.1002/9783527664573.ch8
Autor:
Carmen Nájera, Marie‐Noelle Roy
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[2592-95-2] (C15H13N3O)n (MW 251.28) (polystyrene-divinylbenzene (ca. 1 mol %) copolymer resin; reagent used for peptide coupling) Alternate Name: PS-HOBt, PS-HOBT. Solubility: insoluble in all solvents; polymer swells in DMF, CH2Cl2, and CH3CN. Form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ddd24c214447f35c9aa8ba4d1128981
https://doi.org/10.1002/047084289x.rn00265.pub2
https://doi.org/10.1002/047084289x.rn00265.pub2
Autor:
Marie‐Noelle Roy
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
(Ethyl 2-(diphenoxyphosphinyl) acetate) [16139-79-0] C16H17O5P (MW: 320.28) InChI = 1S/C16H17O5P/c1-2-19-16(17)13-22(18,20-14-9-5-3-6-10-14)21-15-11-7-4-8-12-15/h3-12H,2,13H2,1H3 InChIKey = UQMFCYBSUVRGNU-UHFFFAOYSA-N ((Z)-selective Horner–Wadswort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e743bf21a4a9ebafeaa91116f26afb33
https://doi.org/10.1002/047084289x.rn01590
https://doi.org/10.1002/047084289x.rn01590
Autor:
Marie‐Noelle Roy, Noboru Ono
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[4749-28-4] C3H5NO2 (MW 87.09) InChI = 1S/C3H5NO2/c1-3(2)4(5)6/h1H2,2H3 InChIKey = GXEXLSDIVMVEFZ-UHFFFAOYSA-N (Michael addition to afford 1,4-diketones,4 furans,7 and pyrroles,11 and an electrophilic reagent for α-keto cation in the Friedel–Craft
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4513f348e9ebd80c6857793335d48f90
https://doi.org/10.1002/047084289x.rn053.pub2
https://doi.org/10.1002/047084289x.rn053.pub2
Autor:
Marie‐Noelle Roy, Noboru Ono
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[3156-70-5] C3H5NO2 (MW 87.09) InChI = 1S/C3H5NO2/c1-2-3-4(5)6/h2-3H,1H3 InChIKey = RIHXMHKNTLBIPJ-UHFFFAOYSA-N (Michael addition of various nucleophiles such as organolithium reagents,5, 6 enamines,13, 15, 19 allylstannane,9 and alkyl radicals22) Ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16a24e052722e67ce4ba4eb04560bc67
https://doi.org/10.1002/047084289x.rn052.pub2
https://doi.org/10.1002/047084289x.rn052.pub2
Autor:
Brad DeHoff, Marie‐Noelle Roy
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[88738-78-7] C7H9F6O5P (MW 318.13) InChI = 1S/C7H9F6O5P/c1-16-5(14)2-19(15,17-3-6(8,9)10)18-4-7(11,12)13/h2-4H2,1H3 InChIKey = PVSJXEDBEXYLML-UHFFFAOYSA-N (Horner–Emmons reagent for the production of α,β-unsaturated esters with (Z) selectivity) A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d19b082ac81d027fbfe73be3d061b83f
https://doi.org/10.1002/047084289x.rm145.pub2
https://doi.org/10.1002/047084289x.rm145.pub2